Abstract
Despite tremendous efforts to synthesize isolable compounds with an Si=O bond, silicon analogues of ketones that contain an unperturbed Si=O bond have remained elusive for more than 100 years. Herein, we report the synthesis of an isolable silicon analogue of a ketone that exhibits a three-coordinate silicon center and an unperturbed Si=O bond, thus representing the first example of a genuine silanone. Most importantly, this silanone does not require coordination by Lewis bases and acids and/or the introduction of electron-donating groups to stabilize the Si=O bond. The structure and properties of this unperturbed Si=O bond were examined by a single-crystal X-ray diffraction analysis, NMR spectroscopy, and theoretical calculations. Bimolecular reactions revealed high electrophilicity on the Si atom and high nucleophilicity on the O atom of this genuine Si=O bond.
Original language | English |
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Pages (from-to) | 9425-9428 |
Number of pages | 4 |
Journal | Angewandte Chemie - International Edition |
Volume | 58 |
Issue number | 28 |
DOIs | |
Publication status | Published - 2019 Jul 8 |
Keywords
- carbonyl compounds
- ketones
- Si=O bonds
- silanones
- silicon